That's why it's so distressing to learn of a new drug recall issued by the U.S. Food and Drug Administration (FDA) in which 7,100 bottles of the antidepressant Duloxetine, distributed under the brand name Cymbalta,

The Federal Drug Administration issued a recall on Tuesday for a common medicine for depression. Over 7,000 bottles of Duloxetine were recalled due to the elevated presence of Nitrosamine, an ingredient believed to be cancerous,

The recall covers more than 7,000 bottles of duloxtine, sold as Cymbalta, due to the presence of nitrosamines.